LUC00210I2 - - Google Patents
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- Publication number
- LUC00210I2 LUC00210I2 LU00210C LUC00210C LUC00210I2 LU C00210 I2 LUC00210 I2 LU C00210I2 LU 00210 C LU00210 C LU 00210C LU C00210 C LUC00210 C LU C00210C LU C00210 I2 LUC00210 I2 LU C00210I2
- Authority
- LU
- Luxembourg
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005131161 | 2005-04-28 | ||
| JP2005312076 | 2005-10-27 | ||
| EP06758843.4A EP1874117B8 (en) | 2005-04-28 | 2006-04-28 | Polycyclic carbamoylpyridone derivative having hiv integrase inhibitory activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LUC00210I2 true LUC00210I2 (en) | 2022-10-07 |
Family
ID=37215098
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU92446C LU92446I2 (en) | 2005-04-28 | 2014-05-07 | Dolutegravir or a pharmaceutically acceptable salt or solvate thereof, including sodium dolutegravir |
| LU00210C LUC00210I2 (en) | 2005-04-28 | 2021-06-15 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU92446C LU92446I2 (en) | 2005-04-28 | 2014-05-07 | Dolutegravir or a pharmaceutically acceptable salt or solvate thereof, including sodium dolutegravir |
Country Status (30)
| Country | Link |
|---|---|
| US (22) | US8129385B2 (en) |
| EP (9) | EP2527007B1 (en) |
| JP (2) | JP4295353B2 (en) |
| KR (4) | KR101363875B1 (en) |
| AU (1) | AU2006239177B8 (en) |
| BE (2) | BE2014C038I2 (en) |
| BR (1) | BRPI0610030B8 (en) |
| CA (1) | CA2606282C (en) |
| CY (7) | CY1115151T1 (en) |
| DK (6) | DK3284520T3 (en) |
| EA (1) | EA014162B1 (en) |
| ES (7) | ES2743531T3 (en) |
| FI (1) | FIC20210017I1 (en) |
| FR (2) | FR14C0041I2 (en) |
| HK (2) | HK1249742A1 (en) |
| HU (6) | HUE044978T2 (en) |
| IL (4) | IL186555A (en) |
| LT (5) | LT3372281T (en) |
| LU (2) | LU92446I2 (en) |
| MA (1) | MA29460B1 (en) |
| MX (2) | MX302718B (en) |
| NL (2) | NL300676I2 (en) |
| NO (5) | NO339525B1 (en) |
| NZ (1) | NZ562339A (en) |
| PL (5) | PL2465580T3 (en) |
| PT (5) | PT1874117E (en) |
| SI (6) | SI3187225T1 (en) |
| TW (1) | TWI378931B (en) |
| VN (1) | VN34404A1 (en) |
| WO (1) | WO2006116764A1 (en) |
Families Citing this family (153)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2422444C2 (en) | 2003-12-24 | 2011-06-27 | Байота Сайентифик Менеджмент Пти Лтд | Polycyclic agents for treating respiratory syncytial viral infections |
| US7273859B2 (en) * | 2004-05-12 | 2007-09-25 | Bristol-Myers Squibb Company | HIV integrase inhibitors: cyclic pyrimidinone compounds |
| PT1874117E (en) * | 2005-04-28 | 2013-10-17 | Shionogi & Co | Polycyclic carbamoylpyridone derivative having hiv integrase inhibitory activity |
| CA2607151C (en) | 2005-05-10 | 2012-06-19 | Merck & Co., Inc. | Hiv integrase inhibitors |
| CA2622639C (en) | 2005-10-04 | 2012-01-03 | Istituto Di Recerche Di Biologia Molecolare P. Angeletti S.P.A. | Hiv integrase inhibitors |
| AU2006307101A1 (en) * | 2005-10-27 | 2007-05-03 | Shionogi & Co., Ltd. | Polycyclic carbamoylpyridone derivative having inhibitory activity on HIV integrase |
| TWI423972B (en) | 2006-09-28 | 2014-01-21 | Biota Scient Management | Polycyclic agents for the treatment of respiratory syncytial virus infections |
| HRP20120328T2 (en) | 2007-11-15 | 2012-09-30 | Gilead Sciences | Inhibitors of human immunodeficiency virus replication |
| EP2574610A1 (en) * | 2007-11-15 | 2013-04-03 | Gilead Sciences, Inc. | Inhibitors of human immonodeficiency virus replication |
| WO2009062285A1 (en) | 2007-11-16 | 2009-05-22 | Boehringer Ingelheim International Gmbh | Inhibitors of human immunodeficiency virus replication |
| WO2010011818A1 (en) * | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
| CN103951643B (en) * | 2008-07-25 | 2015-12-09 | 盐野义制药株式会社 | As the compound of hiv integrase inhibitor |
| SI2320908T1 (en) | 2008-07-25 | 2014-05-30 | Viiv Healthcare Company | Dolutegravir Prodrugs |
| JP5551697B2 (en) * | 2008-07-25 | 2014-07-16 | ビーブ・ヘルスケア・カンパニー | Compound |
| WO2010011815A1 (en) * | 2008-07-25 | 2010-01-28 | Smithkline Beecham Corporation | Chemical compounds |
| KR101733625B1 (en) * | 2008-12-11 | 2017-05-10 | 시오노기세야쿠 가부시키가이샤 | Synthesis of carbamoylpyridone hiv integrase inhibitors and intermediates |
| AU2014277831C1 (en) * | 2008-12-11 | 2022-10-06 | Shionogi & Co. Ltd. | Synthesis of carbamoylpyridone hiv integrase inhibitors and intermediates |
| KR101678563B1 (en) | 2008-12-11 | 2016-11-22 | 비이브 헬쓰케어 컴퍼니 | Processes and intermediates for carbamoylpyridone hiv integrase inhibitors |
| KR101663222B1 (en) * | 2008-12-11 | 2016-10-06 | 시오노기세야쿠 가부시키가이샤 | Maltol ether processes and intermediates |
| TWI518084B (en) | 2009-03-26 | 2016-01-21 | 鹽野義製藥股份有限公司 | Process for pyrone and pyridone derivatives |
| DK2444400T3 (en) | 2009-06-15 | 2018-06-18 | Shionogi & Co | SUBSTITUTED POLYCYCLIC CARBAMOYLPYRIDONE DERIVATIVE |
| WO2011011483A1 (en) * | 2009-07-22 | 2011-01-27 | Glaxosmithkline Llc | Chemical compounds |
| JP5624148B2 (en) | 2009-10-13 | 2014-11-12 | エランコ・アニマル・ヘルス・アイルランド・リミテッド | Macrocyclic integrase inhibitor |
| AU2014202406C1 (en) * | 2010-01-27 | 2019-03-07 | Viiv Healthcare Company | Antiviral therapy |
| UA105556C2 (en) * | 2010-01-27 | 2014-05-26 | Віів Гелскер Компані | Combination of compounds comprising hiv integrase inhibitors with other therapeutical agents |
| AU2014202404C1 (en) * | 2010-01-27 | 2022-06-23 | Viiv Healthcare Company | Antiviral therapy |
| TWI508968B (en) | 2010-02-08 | 2015-11-21 | Biota Scient Management | Compounds for treating respiratory syncytial virus infections |
| MX2012009869A (en) * | 2010-02-26 | 2012-09-12 | Japan Tobacco Inc | DERIVED FROM 1, 3,4, 8-TETRAHIDRO-2H-PIRIDO [1, 2-A] PIRAZINA AND ITS USE AS AN INHIBITOR OF THE INTEGRESS OF HIV. |
| TWI582097B (en) | 2010-03-23 | 2017-05-11 | Viiv醫療保健公司 | Process for preparing carbamoylpyridone derivatives and intermediates |
| RU2567385C2 (en) | 2010-04-02 | 2015-11-10 | ЯНССЕН Ар ЭНД Ди АЙРЛЭНД | Macrocyclic integrase inhibitors |
| JP5766690B2 (en) * | 2010-04-12 | 2015-08-19 | 塩野義製薬株式会社 | Pyridone derivatives having integrase inhibitory activity |
| WO2012006104A2 (en) | 2010-06-28 | 2012-01-12 | Academia Sinica, Taiwan | Compounds and methods for treating tuberculosis infection |
| PT2602260T (en) | 2010-08-05 | 2016-12-27 | Shionogi & Co | Process for preparing compound having hiv integrase inhibitory activity |
| TWI577377B (en) * | 2010-09-16 | 2017-04-11 | Viiv醫療保健公司 | Pharmaceutical composition |
| CA2812363C (en) | 2010-09-24 | 2019-04-02 | Shionogi & Co., Ltd. | Substituted polycyclic carbamoyl pyridone derivative prodrug |
| US8796303B2 (en) | 2010-11-26 | 2014-08-05 | Biota Scientific Management Pty Ltd. | Imidazo[2,1-G][1,7]naphthyridines for treating respiratory syncytial virus infections |
| WO2012151361A1 (en) * | 2011-05-03 | 2012-11-08 | Concert Pharmaceuticals Inc. | Carbamoylpyridone derivatives |
| US9206197B2 (en) | 2011-09-14 | 2015-12-08 | Mapi Pharma Ltd. | Amorphous form of dolutegravir |
| CA2851218A1 (en) | 2011-10-12 | 2013-04-18 | Shionogi & Co., Ltd. | Polycyclic pyridone derivative having integrase-inhibiting activity |
| WO2013102145A1 (en) | 2011-12-28 | 2013-07-04 | Global Blood Therapeutics, Inc. | Substituted heteroaryl aldehyde compounds and methods for their use in increasing tissue oxygenation |
| DK3738434T3 (en) | 2011-12-28 | 2023-12-04 | Global Blood Therapeutics Inc | Intermediates for obtaining substituted benzaldehyde compounds and methods for using them in increasing tissue oxygenation |
| WO2014099586A1 (en) | 2012-12-17 | 2014-06-26 | Merck Sharp & Dohme Corp. | 4-pyridinonetriazine derivatives as hiv integrase inhibitors |
| CA2893843C (en) * | 2012-12-21 | 2018-09-04 | Gilead Sciences, Inc. | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
| HK1214817A1 (en) * | 2012-12-27 | 2016-08-05 | Japan Tobacco Inc. | Substituted spiropyrido[1,2-a]pyrazine derivative and medicinal use thereof as hiv integrase inhibitor |
| EP2956123A1 (en) | 2013-02-18 | 2015-12-23 | ratiopharm GmbH | Solid pharmaceutical dosage form of dolutegravir |
| EP2767272A1 (en) | 2013-02-18 | 2014-08-20 | Ratiopharm GmbH | Solid pharmaceutical dosage form of dolutegravir |
| US9573965B2 (en) | 2013-02-19 | 2017-02-21 | Aurobindo Pharma Ltd | Process for the preparation of Dolutegravir |
| KR102280614B1 (en) | 2013-03-15 | 2021-07-21 | 글로벌 블러드 테라퓨틱스, 인크. | Compounds and uses thereof for the modulation of hemoglobin |
| US9422279B2 (en) | 2013-03-15 | 2016-08-23 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US9458139B2 (en) | 2013-03-15 | 2016-10-04 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US10100043B2 (en) | 2013-03-15 | 2018-10-16 | Global Blood Therapeutics, Inc. | Substituted aldehyde compounds and methods for their use in increasing tissue oxygenation |
| AU2014237330A1 (en) | 2013-03-15 | 2015-09-17 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| BR112015021982B1 (en) | 2013-03-15 | 2022-12-13 | Global Blood Therapeutics, Inc | COMPOUNDS AND THEIR USES FOR HEMOGLOBIN MODULATION |
| US20140274961A1 (en) | 2013-03-15 | 2014-09-18 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US9604999B2 (en) | 2013-03-15 | 2017-03-28 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US10266551B2 (en) | 2013-03-15 | 2019-04-23 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US9802900B2 (en) | 2013-03-15 | 2017-10-31 | Global Blood Therapeutics, Inc. | Bicyclic heteroaryl compounds and uses thereof for the modulation of hemoglobin |
| US8952171B2 (en) | 2013-03-15 | 2015-02-10 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| WO2014172188A2 (en) | 2013-04-16 | 2014-10-23 | Merck Sharp & Dohme Corp. | 4-pyridone derivative compounds and uses thereof as hiv integrase inhibitors |
| WO2014200880A1 (en) * | 2013-06-13 | 2014-12-18 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds as hiv integrase inhibitors |
| EP3016935B1 (en) * | 2013-07-04 | 2018-09-05 | Hetero Research Foundation | Process for the preparation of intermediate of dolutegravir |
| NO2865735T3 (en) | 2013-07-12 | 2018-07-21 | ||
| DK3019503T3 (en) | 2013-07-12 | 2017-11-20 | Gilead Sciences Inc | POLYCYCLIC-CARBAMOYLPYRIDON COMPOUNDS AND ITS USES FOR TREATING HIV INFECTIONS |
| EP3022209B1 (en) | 2013-07-17 | 2018-03-07 | ratiopharm GmbH | Dolutegravir potassium salt |
| WO2015019310A1 (en) | 2013-08-07 | 2015-02-12 | Mylan Laboratories Ltd | Process for the preparation of dolute-gravir and intermediates thereof |
| WO2015039348A1 (en) * | 2013-09-23 | 2015-03-26 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds useful as hiv integrase inhibitors |
| MX367057B (en) | 2013-09-27 | 2019-08-02 | Merck Sharp & Dohme | Substituted quinolizine derivatives useful as hiv integrase inhibitors. |
| EA201992707A1 (en) | 2013-11-18 | 2020-06-30 | Глобал Блад Терапьютикс, Инк. | COMPOUNDS AND THEIR APPLICATIONS FOR HEMOGLOBIN MODULATION |
| WO2015092752A1 (en) | 2013-12-20 | 2015-06-25 | Mylan Laboratories Ltd. | Novel crystalline form of dolutegravir sodium |
| WO2015089847A1 (en) * | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | Spirocyclic heterocycle compounds useful as hiv integrase inhibitors |
| WO2015108945A2 (en) | 2014-01-14 | 2015-07-23 | Board Of Regents Of The University Of Nebraska | Compositions and methods for the delivery of therapeutics |
| IN2014CH00247A (en) | 2014-01-21 | 2015-08-14 | Laurus Labs Private Ltd | |
| SI3102208T2 (en) | 2014-02-07 | 2024-10-30 | Global Blood Therapeutics, Inc. | Crystalline polymorph of the free base of 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde |
| CN107056813B (en) * | 2014-03-19 | 2019-07-30 | 杭州普晒医药科技有限公司 | The crystal form of degevir sodium salt and its preparation method |
| WO2015140569A1 (en) | 2014-03-20 | 2015-09-24 | Cipla Limited | Pharmaceutical composition |
| ZA201503540B (en) * | 2014-05-20 | 2016-10-26 | Cipla Ltd | Process for preparing polycyclic carbamoyl pyridone derivatives |
| NO2717902T3 (en) * | 2014-06-20 | 2018-06-23 | ||
| TW201613936A (en) | 2014-06-20 | 2016-04-16 | Gilead Sciences Inc | Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide |
| TWI677489B (en) * | 2014-06-20 | 2019-11-21 | 美商基利科學股份有限公司 | Synthesis of polycyclic-carbamoylpyridone compounds |
| EP3757105B1 (en) | 2014-08-22 | 2024-07-24 | Shionogi & Co., Ltd. | Polycyclic pyridone derivative having integrase inhibitory activity |
| US11311545B2 (en) | 2014-10-09 | 2022-04-26 | Board Of Regents Of The University Of Nebraska | Compositions and methods for the delivery of therapeutics |
| WO2016092527A1 (en) * | 2014-12-12 | 2016-06-16 | Sun Pharmaceutical Industries Limited | A process for the preparation of dolutegravir |
| TWI738321B (en) | 2014-12-23 | 2021-09-01 | 美商基利科學股份有限公司 | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
| WO2016102078A1 (en) | 2014-12-24 | 2016-06-30 | Ratiopharm Gmbh | Solid state forms of dolutegravir sodium |
| EP3045461A1 (en) | 2015-01-16 | 2016-07-20 | LEK Pharmaceuticals d.d. | Processes for preparing dolutegravir and analogues thereof |
| EP3253767A2 (en) | 2015-02-06 | 2017-12-13 | Mylan Laboratories Ltd. | Processes for the preparation of dolute-gravir |
| CZ201599A3 (en) | 2015-02-13 | 2016-08-24 | Zentiva, K.S. | Solid forms of dolutegravir salts and process for preparing thereof |
| US10081647B2 (en) * | 2015-03-26 | 2018-09-25 | Merck Sharp & Dohme Corp. | Phosphate substituted quinolizine derivatives useful as HIV integrase inhibitors |
| MA41841A (en) | 2015-03-30 | 2018-02-06 | Global Blood Therapeutics Inc | ALDEHYDE COMPOUNDS FOR THE TREATMENT OF PULMONARY FIBROSIS, HYPOXIA, AND AUTOIMMUNE AND CONNECTIVE TISSUE DISEASES |
| TR201905009T4 (en) | 2015-04-02 | 2019-05-21 | Gilead Sciences Inc | Polycyclic-carbamoylpyridone compounds and their pharmaceutical uses. |
| DK4219508T3 (en) * | 2015-04-28 | 2024-08-05 | Shionogi & Co | Substituted polycyclic pyridone derivative and prodrug thereof |
| WO2016187788A1 (en) | 2015-05-25 | 2016-12-01 | Merck Sharp & Dohme Corp. | Fused tricyclic heterocyclic compounds useful for treating hiv infection |
| CZ2015537A3 (en) | 2015-08-04 | 2017-02-15 | Zentiva, K.S. | Solid forms of the amorphous dolutegravir |
| US10597404B2 (en) | 2015-08-19 | 2020-03-24 | Laurus Labs Ltd. | Polymorphs of dolutegravir and salts thereof |
| SI3346995T1 (en) | 2015-11-09 | 2019-11-29 | Gilead Sciences Inc | Therapeutic composition for the treatment of human immunodeficiency virus |
| WO2017087257A1 (en) | 2015-11-17 | 2017-05-26 | Merck Sharp & Dohme Corp. | Amido-substituted pyridotriazine derivatives useful as hiv integrase inhibitors |
| US11020382B2 (en) | 2015-12-04 | 2021-06-01 | Global Blood Therapeutics, Inc. | Dosing regimens for 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde |
| WO2017106071A1 (en) | 2015-12-15 | 2017-06-22 | Merck Sharp & Dohme Corp. | Spirocyclic quinolizine derivatives useful as hiv integrase inhibitors |
| US10696636B2 (en) | 2015-12-21 | 2020-06-30 | Lupin Limited | Process for the preparation of HIV integrase inhibitors |
| AR108435A1 (en) | 2016-05-12 | 2018-08-22 | Global Blood Therapeutics Inc | PROCESS TO SYNTHETIZE 2-HYDROXI-6 - ((2- (1-ISOPROPIL-1H-PIRAZOL-5-IL) -PIRIDIN-3-IL) METOXI) BENZALDEHYDE |
| WO2017208105A1 (en) | 2016-05-30 | 2017-12-07 | Lupin Limited | Novel crystalline form of dolutegravir sodium |
| ES3035041T3 (en) | 2016-06-23 | 2025-08-27 | Viiv Healthcare Co | Compositions and methods for the delivery of therapeutics |
| US11045423B2 (en) | 2016-08-08 | 2021-06-29 | Hetero Labs Limited | Anti-retroviral compositions |
| US20190175511A1 (en) | 2016-08-08 | 2019-06-13 | Hetero Labs Limited | A Multi-Class Anti-Retroviral Composition |
| CN109789144B (en) * | 2016-08-12 | 2022-04-15 | 马德拉医疗公司 | Protein kinase modulators |
| WO2018042332A1 (en) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinations and uses and treatments thereof |
| US20190216725A1 (en) * | 2016-09-21 | 2019-07-18 | Merck Shapr & Dohme Corp. | Drug delivery system for the delivery of integrase inhibitors |
| TWI778983B (en) | 2016-10-12 | 2022-10-01 | 美商全球血液治療公司 | Tablets comprising 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde |
| JOP20190130A1 (en) | 2016-12-02 | 2019-06-02 | Merck Sharp & Dohme | Tetracyclic heterocyclic compounds useful as integrated enzyme inhibitors for human immunodeficiency virus (HIV) |
| AU2017367714B2 (en) | 2016-12-02 | 2020-11-12 | Merck Sharp & Dohme Corp. | Tricyclic heterocycle compounds useful as HIV integrase inhibitors |
| WO2018109786A1 (en) | 2016-12-16 | 2018-06-21 | Cipla Limited | Novel polymoprphs and salts of polycyclic carbamoyl pyridone derivatives |
| WO2018140368A1 (en) | 2017-01-26 | 2018-08-02 | Merck Sharp & Dohme Corp. | Substituted quinolizine derivatives useful as hiv integrase inhibitors |
| CA3053202C (en) * | 2017-02-16 | 2022-10-04 | Sandoz Ag | Crystalline forms of cabotegravir sodium |
| EP3363802B1 (en) | 2017-02-16 | 2019-11-20 | Sandoz AG | Crystalline form of cabotegravir sodium |
| WO2019016679A1 (en) * | 2017-07-18 | 2019-01-24 | Viiv Healthcare Company | COMBINATION THERAPY |
| KR20260015342A (en) | 2017-07-21 | 2026-02-02 | 비이브 헬쓰케어 컴퍼니 | Regimens for treating hib infections and aids |
| US20210040116A1 (en) | 2017-09-07 | 2021-02-11 | Cipla Limited | New Polymorphs of Dolutegravir Sodium |
| AU2018344739B2 (en) | 2017-10-06 | 2023-04-13 | Shionogi & Co., Ltd. | Stereoselective process for preparing substituted polycyclic pyridone derivatives |
| US11839623B2 (en) | 2018-01-12 | 2023-12-12 | Board Of Regents Of The University Of Nebraska | Antiviral prodrugs and formulations thereof |
| WO2019159199A1 (en) | 2018-02-16 | 2019-08-22 | Cipla Limited | Continues flow process for the preparation of active pharmaceutical ingredients - polycyclic carbamoyl pyridone derivatives and intermediates thereof |
| US11458136B2 (en) | 2018-04-09 | 2022-10-04 | Board Of Regents Of The University Of Nebraska | Antiviral prodrugs and formulations thereof |
| CN110526930B (en) | 2018-05-23 | 2022-06-03 | 莫云芬 | anti-HIV (human immunodeficiency virus) sulfur-containing polycyclic-hydroxypyridone formamide analogue and application thereof |
| TWI820141B (en) * | 2018-05-31 | 2023-11-01 | 日商鹽野義製藥股份有限公司 | Polycyclic pyridotriazine derivative |
| US11453669B2 (en) | 2018-05-31 | 2022-09-27 | Shionogi & Co., Ltd. | Polycyclic pyridone derivative |
| CA3102063A1 (en) | 2018-05-31 | 2019-12-05 | Shionogi & Co., Ltd. | Polycyclic carbamoylpyridone derivative |
| WO2020012408A2 (en) | 2018-07-12 | 2020-01-16 | Laurus Labs Limited | A process for purification of protected polycyclic carbamoylpyridone derivatives |
| EP3860975B1 (en) | 2018-10-01 | 2023-10-18 | Global Blood Therapeutics, Inc. | Modulators of hemoglobin for the treatment of sickle cell disease |
| EP4234560A3 (en) | 2018-10-22 | 2023-09-13 | Board of Regents of the University of Nebraska | Antiviral prodrugs and nanoformulations thereof |
| CN113382737B (en) | 2018-11-29 | 2025-06-03 | 内布拉斯加大学董事会 | Antiviral prodrugs and their nanoparticle preparations |
| IL286328B1 (en) | 2019-03-22 | 2026-04-01 | Gilead Sciences Inc | Bridged tricyclic carbamoylpyridone compounds and their pharmaceutical use |
| RU2717101C1 (en) * | 2019-06-03 | 2020-03-18 | Андрей Александрович Иващенко | Anellated 9-hydroxy-1,8-dioxo-1,3,4,8-tetrahydro-2h-pyrido[1,2-a]pyrazine-7-carboxamides - integrase inhibitors, methods for preparing and using thereof |
| US20200398978A1 (en) | 2019-06-20 | 2020-12-24 | Bell Helicopter Textron Inc. | Low-drag rotor blade extension |
| US11248005B2 (en) | 2019-07-08 | 2022-02-15 | Lupin Limited | Process for preparation of intermediates used for the synthesis of HIV integrase inhibitor |
| US12577241B2 (en) | 2019-11-28 | 2026-03-17 | Shionogi & Co., Ltd. | Polycyclic pyridopyrazine derivative |
| EP4066839A4 (en) | 2019-11-28 | 2023-12-27 | Shionogi & Co., Ltd | Prophylactic and therapeutic pharmaceutical agent for hiv infectious diseases characterized by comprising combination of integrase inhibitor and anti-hiv agent |
| CA3164528A1 (en) | 2019-12-09 | 2021-06-17 | Viiv Healthcare Company | Pharmaceutical compositions comprising cabotegravir |
| CR20220418A (en) | 2020-02-24 | 2022-10-10 | Gilead Sciences Inc | Tetracyclic compounds for treating hiv infection |
| WO2025068743A1 (en) | 2023-09-27 | 2025-04-03 | ViiV Healthcare UK (No.3) Limited | Pharmaceutical composition of cabotegravir |
| US20230218644A1 (en) | 2020-04-16 | 2023-07-13 | Som Innovation Biotech, S.A. | Compounds for use in the treatment of viral infections by respiratory syndrome-related coronavirus |
| WO2022051198A1 (en) | 2020-09-01 | 2022-03-10 | Viiv Healthcare Company | Combination of cabotegravir and levonorgestrel |
| CA3192145A1 (en) | 2020-09-30 | 2022-04-07 | Gilead Sciences, Inc. | Bridged tricyclic carbamoylpyridone compounds and uses thereof |
| WO2022079739A1 (en) | 2020-10-14 | 2022-04-21 | Cipla Limited | Fixed dose compositions of cabotegravir and rilpivirine |
| JP2024500322A (en) | 2020-12-07 | 2024-01-09 | ヴィーブ、ヘルスケア、カンパニー | combination therapy |
| JP7591155B2 (en) | 2021-01-19 | 2024-11-27 | ギリアード サイエンシーズ, インコーポレイテッド | Substituted pyridotriazine compounds and uses thereof |
| CN117715908A (en) | 2021-06-03 | 2024-03-15 | 江苏恒瑞医药股份有限公司 | Pyridone compounds having integrase inhibitory activity and their pharmaceutical use |
| CN114230579A (en) * | 2021-11-12 | 2022-03-25 | 南京艾迪医药科技有限公司 | Polycyclic carbamoylpyridone derivatives, process for their preparation and pharmaceutical compositions containing them |
| EP4441238A1 (en) | 2021-12-03 | 2024-10-09 | VIIV Healthcare Company | Process of synthesizing (r)-3-aminobutan-1-ol |
| TWI856796B (en) | 2022-04-06 | 2024-09-21 | 美商基利科學股份有限公司 | Bridged tricyclic carbamoylpyridone compounds and uses thereof |
| EP4619400A4 (en) * | 2023-01-18 | 2026-03-25 | Ascletis Bioscience Co Ltd | Integrase inhibitors and their use |
| CN121909019A (en) | 2023-09-27 | 2026-04-21 | Viiv保健英国第三有限公司 | Pharmaceutical composition |
| WO2025128496A1 (en) | 2023-12-12 | 2025-06-19 | Viiv Healthcare Company | Crystalline form |
| WO2025128498A1 (en) | 2023-12-12 | 2025-06-19 | Viiv Healthcare Company | Pharmaceutical compositions |
| TW202602442A (en) | 2024-03-01 | 2026-01-16 | 英商Viiv醫療保健英國(No 3)有限公司 | Dosing regimen |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3959316A (en) * | 1972-03-13 | 1976-05-25 | Snam Progetti S.P.A. | Procedure for propylene oxide synthesis |
| JPH0296506A (en) * | 1988-09-30 | 1990-04-09 | Daicel Chem Ind Ltd | Herbicide composition |
| JP2533796B2 (en) | 1988-10-18 | 1996-09-11 | ダイセル化学工業株式会社 | 5-Alkoxypyridine-3-carboxamide derivative, method for producing the same, and plant growth inhibitor |
| JP2551472B2 (en) * | 1988-10-18 | 1996-11-06 | ダイセル化学工業株式会社 | 5-Alkoxy-γ-pyrone-3-carboxamide derivative, method for producing the same, and plant growth inhibitor |
| RU2220960C2 (en) | 1997-12-22 | 2004-01-10 | Фармация Энд Апджон Компани | 4-hydroxy-3-quinolinecarboxamides and hydrazides, pharmaceutical composition and treatment method based on thereof |
| AU2001262732A1 (en) † | 2000-06-14 | 2001-12-24 | Shionogi And Co., Ltd. | Inhibitor for enzyme having two divalent metal ions as active centers |
| US6580562B2 (en) | 2000-07-24 | 2003-06-17 | Yazaki Corporation | On-vehicle display unit |
| US6384263B1 (en) | 2000-08-04 | 2002-05-07 | E. I. Du Pont De Nemours And Company | Process for making 3-hydroxyalkanelnitriles and conversion of the 3-hydroxyalkanelnitrile to an hydroxyaminoalkane |
| AU1532802A (en) | 2000-10-12 | 2002-04-22 | Merck & Co Inc | Aza- and polyaza-naphthalenyl-carboxamides useful as hiv integrase inhibitors |
| JP2003032772A (en) | 2001-07-12 | 2003-01-31 | Foster Electric Co Ltd | Earphone |
| DK3042894T1 (en) | 2001-08-10 | 2016-11-07 | Shionogi & Co | ANTIVIRAL AGENT |
| SI1441734T1 (en) | 2001-10-26 | 2007-08-31 | Angeletti P Ist Richerche Bio | Dihydroxypyrimidine carboxamide inhibitors of hiv integrase |
| DE60209381T2 (en) | 2001-10-26 | 2006-10-05 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | N-SUBSTITUTED HYDROXYPYRIMIDINONE CARBOXAMIDE INHIBITORS OF THE HIV INTEGRASE |
| ES2291642T3 (en) | 2002-01-17 | 2008-03-01 | MERCK & CO., INC. | USEFUL HYDROXINE FTIRIDINON CARBOXAMIDS AS INHIBITORS OF HIV INTEGRESS. |
| AU2003248872A1 (en) | 2002-07-09 | 2004-01-23 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
| DE60322920D1 (en) | 2002-08-13 | 2008-09-25 | Shionogi & Co | HETEROCYCLIC COMPOUNDS WITH HIV INTEGRATE-INHIBITOR EFFECT |
| US7517532B2 (en) * | 2002-09-11 | 2009-04-14 | Merck & Co., Inc. | Dihydroxypyridopyrazine-1,6-dione compounds useful as HIV integrase inhibitors |
| BR0317749A (en) | 2002-12-27 | 2005-11-22 | Angeletti P Ist Richerche Bio | Compound, pharmaceutical composition, and use of a compound |
| US6960680B2 (en) | 2003-01-08 | 2005-11-01 | Rhodia Chirex, Inc. | Manufacture of water-soluble β-hydroxynitriles |
| JP2004244320A (en) | 2003-02-10 | 2004-09-02 | Shionogi & Co Ltd | Nitrogen-containing heterocyclic antiviral agents |
| WO2004101512A2 (en) | 2003-05-13 | 2004-11-25 | Smithkline Beecham Corporation | Naphthyridine integrase inhibitors |
| AU2003273190A1 (en) * | 2003-08-12 | 2005-02-25 | Rachel Beijer | Scheduled message service |
| TW200510425A (en) | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
| JP4530642B2 (en) | 2003-10-31 | 2010-08-25 | オリンパス株式会社 | Endoscope device |
| EP1720856B1 (en) | 2004-02-11 | 2013-08-14 | GlaxoSmithKline LLC | Hiv integrase inhibitors |
| JP2007528394A (en) | 2004-03-09 | 2007-10-11 | メルク エンド カムパニー インコーポレーテッド | HIV integrase inhibitor |
| CA2557926A1 (en) | 2004-03-09 | 2005-09-22 | Monica Donghi | Hiv integrase inhibitors |
| EP1756114B1 (en) | 2004-05-07 | 2014-11-19 | Merck Sharp & Dohme Corp. | Hiv integrase inhibitors |
| WO2006066414A1 (en) | 2004-12-23 | 2006-06-29 | Virochem Pharma Inc. | Hydroxydihydropyridopy razine-1,8-diones and methods for inhibiting hiv integrase |
| ATE516026T1 (en) | 2005-02-21 | 2011-07-15 | Shionogi & Co | BICYCLIC CARBAMOYLPYRIDONE DERIVATIVE WITH HIV INTEGRASE INHIBITING EFFECT |
| AU2006228278C1 (en) | 2005-03-31 | 2011-06-23 | Msd Italia S.R.L. | HIV integrase inhibitors |
| PT1874117E (en) * | 2005-04-28 | 2013-10-17 | Shionogi & Co | Polycyclic carbamoylpyridone derivative having hiv integrase inhibitory activity |
| JP2005312076A (en) | 2005-05-26 | 2005-11-04 | Olympus Corp | Electronic imaging device |
| EP1910363A4 (en) | 2005-08-04 | 2010-05-26 | Glaxosmithkline Llc | Hiv integrase inhibitors |
| AU2006307101A1 (en) | 2005-10-27 | 2007-05-03 | Shionogi & Co., Ltd. | Polycyclic carbamoylpyridone derivative having inhibitory activity on HIV integrase |
-
2006
- 2006-04-28 PT PT67588434T patent/PT1874117E/en unknown
- 2006-04-28 SI SI200632418T patent/SI3187225T1/en unknown
- 2006-04-28 PT PT17195280T patent/PT3284520T/en unknown
- 2006-04-28 ES ES17195280T patent/ES2743531T3/en not_active Expired - Lifetime
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- 2006-04-28 SI SI200631747T patent/SI2465580T1/en unknown
- 2006-04-28 ES ES12159079.8T patent/ES2567197T3/en not_active Expired - Lifetime
- 2006-04-28 ES ES12159082.2T patent/ES2446324T3/en not_active Expired - Lifetime
- 2006-04-28 KR KR1020077027734A patent/KR101363875B1/en not_active Expired - Lifetime
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- 2006-04-28 WO PCT/US2006/016604 patent/WO2006116764A1/en not_active Ceased
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2015
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2016
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2017
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2018
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2019
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2020
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2021
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2022
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2023
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2024
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